Magnetic disk and method for manufacturing same

ABSTRACT

Provided is a method of manufacturing a magnetic disk comprising a granular magnetic recording layer which causes less noise even with a recording capacity thereof of 250 G or more bits per square inch; and a method for manufacturing the same. The magnetic disk according to the present invention comprises: a granular magnetic recording layer ( 20 ) which is formed on a disk substrate  10  directly or via an intermediate layer and which has non-magnetic regions between granular columnar particles; and an auxiliary recording layer ( 22 ) which is formed on the granular magnetic recording layer  20  and which causes exchange interaction among the granular columnar particles, wherein the auxiliary recording layer ( 22 ) contains 0.1 to 3 moles of oxygen.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 13/133,124, filed on Jun. 6, 2011, which is a National Stage of International Application No. PCT/JP2009/070499 filed Dec. 7, 2009, claiming priority to Japanese Patent Application Nos. 2008-311120, filed Dec. 5, 2008 and 2009-087762, filed Mar. 31, 2009 which are hereby incorporated by reference in their entirety.

TECHNICAL FIELD

The present invention relates to a magnetic disk having a carbon-based protective layer and mounted in a hard disk drive (HDD) of a perpendicular magnetic recording system or the like, and a method for manufacturing the same.

BACKGROUND ART

Characteristics required for a magnetic disk mounted in an HDD of a magnetic recording system or the like include, for example, a good SNR of a recorded signal, good thermal stability, and easiness to record. Among others, in order to improve a SNR, it is necessary to reduce the particle diameter of magnetic particles constituting a magnetic recording layer. However, if the particle diameter of magnetic particles is reduced, a signal becomes thermally unstable. In order to thermally stabilize a signal, it is necessary to increase perpendicular magnetic anisotropy energy (Ku), however, if perpendicular magnetic anisotropy energy is increased too much, it becomes impossible to record information on a magnetic head.

In order to solve such a problem, for example, a CGC (Continuous Granular Coupled) medium has been developed, which comprises a granular magnetic recording layer composed of granular columnar particles and non-magnetic regions between the granular columnar particles; and an auxiliary recording layer formed on the granular magnetic recording layer and causing exchange coupling among the granular columnar particles. In the CGC medium, static magnetic characteristics (SNR), recording characteristics, and thermal stability can be controlled by adjusting the exchange interaction between the auxiliary recording layer and the granular magnetic recording layer, and the exchange interaction among the granular columnar particles via the auxiliary recording layer.

PRIOR ART DOCUMENT Patent Document

-   Patent Document 1: Japanese Unexamined Patent Application     Publication No. 2008-84432

SUMMARY OF THE INVENTION Problems to be Solved by the Invention

In a conventional magnetic disk of a perpendicular magnetic recording system, whose recording capacity is less than 250 G bits per square inch, noise can be more reduced when not only a granular magnetic recording layer but also an auxiliary recording layer is provided, as compared with when only a granular magnetic recording layer is provided. However, if the recording capacity is 250 G or more bits per square inch, noise is caused due to strong exchange interaction between magnetic particles in an auxiliary recording layer because the auxiliary recording layer is a continuous film.

One aspect of the present invention was made in view of the above-mentioned problem, and it is an object of the present invention to provide a magnetic disk comprising a granular magnetic recording layer, which causes less noise even with a recording capacity of 250 G or more bits per square inch, and a method for manufacturing the same.

Means for Solving the Problem

One aspect of a magnetic disk according to the present invention comprises: a granular magnetic recording layer which is formed on a disk substrate directly or via an intermediate layer and which has non-magnetic regions between granular columnar particles; and an auxiliary recording layer which is formed on the granular magnetic recording layer and which causes exchange coupling among the granular columnar particles, wherein the auxiliary recording layer contains 0.1 to 3 mol % of oxygen.

In this structure, the auxiliary recording layer containing 0.1 to 3 mol % of oxygen is provided on the magnetic recording layer, and uniformity of the grain boundary among the magnetic particles in the auxiliary recording layer can be thereby improved. As a result, uniformity in magnetic continuity also increases, and consequently noise can be reduced even in a magnetic disk comprising the magnetic recording layer, which has a granular structure and a recording capacity of 250 G or more bits per square inch.

In one aspect of the magnetic disk according to the present invention, the oxygen is preferably contained in the auxiliary recording layer in a state of oxide. Here, the oxide is preferably precipitated on the non-magnetic regions of the granular magnetic recording layer.

In one aspect of the magnetic disk according to the present invention, it is preferable that the granular magnetic recording layer contains oxygen, and that the amount of oxygen contained in the auxiliary recording layer is less than that in the granular magnetic recording layer.

In one aspect of the magnetic disk according to the present invention, the oxygen contained in the granular magnetic recording layer preferably has two or more kinds of oxides mixed therein.

In one aspect of the magnetic disk according to the present invention, a non-magnetic separation layer is preferably interposed between the granular magnetic recording layer and the auxiliary recording layer.

In one aspect of the magnetic disk according to the present invention, the granular magnetic recording layer is preferably composed of two or more layers.

In one aspect of the magnetic disk according to the present invention, the recording capacity is preferably 250 G or more bits per square inch.

Another aspect of a magnetic disk according to the present invention comprises, on a disk substrate, at least: a magnetic recording layer having a granular structure where non-magnetic grain boundary portions are formed between magnetic particles composed of CoCrPt and continuously grow in a columnar shape; and an auxiliary recording layer formed on the magnetic recording layer, wherein the auxiliary recording layer includes: a non-granular auxiliary recording layer which is a magnetic layer almost magnetically continuous in the in-plane direction of the main surface of the disk substrate; and a granular auxiliary recording layer which is provided below the non-granular auxiliary recording layer, has higher coercive force than the non-granular auxiliary recording layer, and has a granular structure.

In this structure, the granular auxiliary recording layer having higher coercive force acts as a pin layer of the non-granular auxiliary recording layer. Therefore, while more blurred writing are generally caused when a thicker auxiliary recording layer is used, a track width can be made narrower (blurred writing can be reduced) and SNR can be improved even if a thicker auxiliary recording layer is provided. Thus, compatibility between a track width and SNR can be achieved.

In another aspect of the magnetic disk according to the present invention, the granular auxiliary recording layer preferably has lower at % of Cr and higher at % of CoPt than the magnetic recording layer. The reason for this is that, in this composition, the granular auxiliary recording layer has higher coercive force than the magnetic recording layer, and ideally acts as a pin layer of the non-granular auxiliary recording layer.

In another aspect of the magnetic disk according to the present invention, the difference (A−B) between a Cr concentration (A) of the magnetic recording layer and a Cr concentration (B) of the granular auxiliary recording layer is preferably not less than 1 at % and not more than 4 at %. That is, compared to the magnetic recording layer, at % of Cr is made smaller and at % of CoPt is made larger to increase coercive force. In other words, in metal layers, the difference (A−B) in Cr concentration (B) is preferably not less than 1 at % and not more than 4 at %.

In another aspect of the magnetic disk according to the present invention, the granular auxiliary recording layer preferably has thinner film thickness than the non-granular auxiliary recording layer. The reason for this is that, if the non-granular auxiliary recording layer is made thinner, recording itself will be impossible, therefore the thickness of the non-granular auxiliary recording layer is maintained to keep OW characteristics, while a blurred writing is prevented by the granular auxiliary recording layer which acts as a pin layer of the non-granular auxiliary recording layer. It is preferable that the film thickness of the granular auxiliary recording layer is 0.5 to 5.0 nm, and that of the non-granular auxiliary recording layer 4.0 to 8.0 nm.

A method for manufacturing a magnetic disk according to the present invention comprises: a magnetic recording layer formation step of forming at least a granular magnetic recording layer on a disk substrate; and an auxiliary recording layer formation step of forming an auxiliary recording layer on the magnetic recording layer, wherein the auxiliary recording layer containing 0.1 to 3 mol % oxygen is formed in the auxiliary recording layer formation step.

In the method for manufacturing the magnetic disk according to the present invention, the auxiliary recording layer is preferably formed by sputtering with use of a sputtering target containing oxide in the auxiliary recording layer formation step.

In the method for manufacturing the magnetic disk according to the present invention, the auxiliary recording layer is preferably formed by reactive sputtering where oxygen is incorporated at a partial pressure of 0.5 to 3% in the auxiliary recording layer formation step.

In the method for manufacturing the magnetic disk according to the present invention, it is preferable that a non-magnetic separation layer is interposed between the granular magnetic recording layer and the auxiliary recording layer so as to control the strength of ferromagnetic coupling between the granular magnetic recording layer and the auxiliary recording layer.

In the method for manufacturing the magnetic disk according to the present invention, the granular magnetic recording layer is preferably formed of two or more layers.

Effect of the Invention

The magnetic disk according to the present invention comprises: a granular magnetic recording layer which is formed on a disk substrate directly or via an intermediate layer and which has non-magnetic regions between granular columnar particles; and an auxiliary recording layer which is formed on the granular magnetic recording layer and which causes exchange coupling among the granular columnar particles, wherein the auxiliary recording layer contains 0.1 to 3 mol % of oxygen, and thereby, less noise is caused even with the recording capacity of 250 G or more bits per square inch.

Moreover, according to the present invention, a perpendicular magnetic recording medium can be provided which can improve recording density by achieving compatibility between a track width and SNR, namely by maintaining the film thickness of the auxiliary recording layer to keep OW characteristics in a good state while narrowing a track width and improving SNR.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a schematic configuration of a magnetic disk according to Embodiment 1 of the present invention.

FIG. 2 illustrates an auxiliary recording layer of the magnetic disk shown in FIG. 1.

FIG. 3 illustrates a configuration of a perpendicular magnetic recording medium according to Embodiment 2 of the present invention.

FIG. 4 illustrates a layer structure from a main recording layer to an auxiliary recording layer of FIG. 3.

FIG. 5 shows comparisons of track widths and SNRs between examples where a granular auxiliary recording layer and a non-granular auxiliary recording layer of a varied film thickness are included and comparative examples where only a non-granular auxiliary recording layer is included.

FIG. 6 illustrates growth of magnetic particles in the case where a magnetic layer which constitutes a magnetic recording layer is formed by a single deposition.

BEST MODES FOR CARRYING OUT THE INVENTION

Preferred embodiments of the present invention will be described in details with reference to the accompanying drawings. The dimensions, materials, and others such as specific numerical values mentioned in these embodiments are merely illustrated to facilitate understanding of the invention, and are not meant to limit the present invention unless otherwise specified. Note that, in the specification and the drawings, components having substantially the same functions and structures are assigned the same reference characters to omit redundant descriptions, and that components not directly relating to the present invention are not shown in the drawings.

Embodiment 1

FIG. 1 shows a schematic configuration of a magnetic disk according to Embodiment 1 of the present invention. A medium of a perpendicular magnetic recording system (a perpendicular magnetic recording medium) 100 shown in FIG. 1 is configured by sequentially laminating a disk substrate 10, an adhesive layer 12, a soft magnetic layer 14, an orientation control layer 16, an underlayer 18, a magnetic recording layer 20, an auxiliary recording layer 22, a medium protective layer 24, and a lubricant layer 26.

For example, a glass substrate, an aluminum substrate, a silicon substrate, or a plastic substrate can be used as the disk substrate (a substrate for a magnetic disk) 10. If a chemically strengthened glass substrate with a smooth surface is used as a substrate 1, the substrate can be manufactured by a manufacturing process including for example: a material processing step and a first lapping step; an end forming step (a coring step of forming a hole, a chamfering step (a chamfered surface forming step) of forming a chamfered surface on an end (an outer peripheral end and/or an inner peripheral end)); an end polishing step (for an outer peripheral end and an inner peripheral end); a second lapping step; a main surface polishing step (first and second polishing steps); and a chemically strengthening step.

The adhesive layer 12 can improve adhesion between the disk substrate 10 and the soft magnetic layer 14, thereby preventing peeling of the soft magnetic layer 14. For example, a CrTi alloy can be used as a material of the adhesive layer 12.

The soft magnetic layer 14 is a layer which causes a magnetic field generated from a main magnetic pole of a magnetic recording head to pass through. Examples of a material constituting the soft magnetic layer 14 include, for example, a CoFeTaZr alloy. In addition, the soft magnetic layer 14 may be configured so that a non-magnetic spacer layer is interposed between a first soft magnetic layer and a second soft magnetic layer to cause AFC (Antiferromagnetic exchange coupling). Thereby, the magnetizing direction of the soft magnetic layer 14 can be aligned along a magnetic path (magnetic circuit) with high accuracy, and the perpendicular components of the magnetizing direction can be extremely reduced, so that less noise can be caused from the soft magnetic layer 14. Here, for example, Ru (ruthenium) can be used as a material of the spacer layer.

The orientation control layer 16 has effects of protecting the soft magnetic layer 14 and of promoting the alignment of the orientation of crystal grains in the underlayer 18. A material of the orientation control layer can be selected from Ni, Cu, Pt, Pd, Zr, Hf, and Nb. Further, the material may be an alloy based on any of the metals and including any one or more of additional elements of Ti, V, Ta, Cr, Mo, and W. For example, NiW, NiCr, a NiTa alloy, a CuW alloy, and a CuCr alloy can be selected suitably. Moreover, the orientation control layer may be formed of two or more layers.

The underlayer 18 has an hcp structure and enables crystals of an hcp structure in the magnetic recording layer 20 to grow into those of a granular structure (of a structure having non-magnetic regions between granular columnar particles). Therefore, as the crystal orientation of the underlayer 18 is higher, the orientation of the magnetic recording layer 20 can be improved. In addition, in order to give separativeness, the underlayer 18 may be formed of a lower layer to which a lower Ar pressure is applied at the time of deposition and an upper layer to which a higher Ar pressure is applied thereat. In addition to Ru, a material of the underlayer can be selected from Re, Pt, a RuCr alloy, a RuCo alloy and the like. Ru has an hcp structure and can satisfactorily orient the Co-based magnetic recording layer. Any oxide may be also added.

The magnetic recording layer 20 is formed on a disk substrate 10 directly or via an intermediate layer. In the magnetic recording layer 20, two or more kinds of oxides (hereinafter referred to as “composite oxides”) are contained, thereby causing the composite oxides to be precipitated in a non-magnetic grain boundary. Namely, Cr and the composite oxides, which are non-magnetic substances, (non-magnetic region 20 a) in the magnetic recording layer 20 are precipitated around Co, which is a magnetic substance, to form the grain boundary, thereby magnetic particles (magnetic grains) 20 b growing in a granular structure of a columnar shape (granular magnetic recording layer).

Here, examples of a material constituting the granular magnetic recording layer include, for example, CoCrPt—SiO₂ (hcp crystal structure), CoCrPt—TiO₂ (hcp crystal structure). Also, the thickness of the magnetic recording layer 20 is preferably 5 to 15 nm.

Moreover, the magnetic recording layer 20 may be formed by laminating two or more thin films. For example, the magnetic recording layer can be formed of two or more layers (lamination film) by depositing any of the above-mentioned materials in multiple times. Thereby, magnetic particles can be prevented from being enlarged as magnetic particles are deposited, and the particle diameters from the lower layer to the upper layer can be made uniform. Note that the same material or different materials may be used as a film to be laminated.

The auxiliary recording layer 22 is formed above the granular magnetic layer, and causes exchange coupling among the granular columnar particles in the granular magnetic layer. The auxiliary recording layer 22 is preferably a thin film (continuous layer) which has high perpendicular magnetic anisotropy and shows high saturation magnetization Ms, and has magnetic continuity in the in-plane direction of the disk substrate. The auxiliary recording layer 22 is intended to improve the reverse magnetic domain nucleus forming magnetic field Hn, thermal fluctuation resistance, and overwrite characteristics. Examples of a material of the auxiliary recording layer 22 include CoCrPtB—CuO, CoCrPtB—CoO, CoCrPtB—Co₃O₄, CoCrPtB—Cr₂O₃, CoCrPtB—SiO₂, and CoCrPtB—TiO₂, as well as other those obtained by adding various oxides to alloys other than CoCrPtB, such as CoPt, CoCrPt, CoCrPtTa, CoCrPtCu, and CoCrPtBCu. Furthermore, the auxiliary recording layer can be formed by reactive sputtering where oxygen is added at a suitable partial pressure at the time of sputtering the alloys.

Furthermore, the auxiliary recording layer 22 contains 0.1 to 3 mol % of oxygen. It is preferable that the amount of oxygen contained in the auxiliary recording layer 22 is less than that in the granular magnetic recording layer 20. With the amounts set up in this way, the auxiliary recording layer 22 can be prevented from being magnetically separated, thereby maintaining an effect as an auxiliary recording layer (effect of making exchange coupling between granular columnar particles). Note that the amount of “oxygen” is calculated in terms of oxygen molecules (O₂). For example, 2 mol % of CuO contain 1 mol of oxygen molecules, and 2 mol % of Si0₂ 2 mol of oxygen molecules.

In the auxiliary recording layer 22, as shown in FIG. 2, oxygen precipitates in a state of oxide, or as a compound obtained by combining oxygen with other atoms. The precipitate 22 a is deposited on the non-magnetic region 20 a of the magnetic recording layer 20. When the auxiliary recording layer 22 is formed by sputtering with use of a sputtering target containing an oxide, oxygen precipitates in a state of oxide. Meanwhile, when the auxiliary recording layer 22 is formed by reactive sputtering where oxygen is incorporated at a partial pressure of 0.5 to 3%, oxygen precipitates as a compound obtained by combining with atoms such as Co or Cr. The thickness of the auxiliary recording layer 22 is preferably 5 to 10 nm. In addition, the auxiliary recording layer 22 may be formed of two or more films.

With 0.1 to 3 mol % of oxygen positively contained in the auxiliary recording layer 22 in this way, structural non-uniformity caused in the course of laminating the auxiliary recording layer can be reduced, and accordingly noise from the auxiliary recording layer resulting from the non-uniformity can be reduced. Furthermore, as a result of the improvement in the characteristics of the auxiliary recording layer, the exchange coupling among the granular columnar particles in the magnetic recording layer 20 can be controlled more easily. Thereby, general noises from the magnetic recording layer 20 to the auxiliary recording layer 22 can be reduced. This effect is remarkable especially in a disk with the recording capacity of 250 G or more bits per square inch.

The medium protective layer 24 is formed by depositing carbon by a CVD method while maintaining a vacuum. The medium protective layer 24 is a protective layer for protecting the perpendicular magnetic recording layer against impacts from a magnetic recording head. In general, as compared with carbon deposited by a sputtering method, carbon deposited by a CVD method has higher film hardness, and thereby can more effectively protect the perpendicular magnetic recording layer against impacts from the magnetic recording head. The thickness of the medium protective layer 24 is preferably 2 to 5 nm.

The lubricant layer 26 is formed by depositing PFPE (perfluoropolyether) by a dip-coating method. Here, the thickness of the lubricant layer 26 is approximately 1 nm.

In the perpendicular magnetic recording medium 100 shown in FIG. 1, a separation layer which is a non-magnetic layer may be interposed between the magnetic recording layer 20 and the auxiliary recording layer 22. With the separation layer interposed, the strength of ferromagnetic exchange coupling between the magnetic recording layer 20 and the auxiliary recording layer 22 can be controlled. As a result, the strength of magnetic coupling between the columnar magnetic particles present in the magnetic recording layer 20 can be also controlled, thereby further improving the medium characteristics. The separation layer can be formed of thin films of Ruthenium (Ru) or a Ru alloy or compound obtained by adding Cr, Co, oxygen or oxide to Ru.

In the manufacturing of the magnetic disk having the above-mentioned configuration, amorphous aluminosilicate glass is first molded in a disk shape by direct-pressing to make a glass disk. Then, the glass disk is sequentially ground, polished, and chemically strengthened to obtain a smooth non-magnetic disk substrate 10 composed of the chemically strengthened glass disk.

On the resultant disk substrate 10, films from the adhesive layer 12 to the auxiliary recording layer 22 are sequentially deposited in an Ar atmosphere by DC magnetron sputtering with use of a vacuumed film forming device, and the medium protective layer 24 is deposited by a CVD method. Then, the lubricant layer 26 is formed by a dip-coating method.

In the deposition of the auxiliary recording layer 22, 0.1 to 3 mol % of oxygen is made contained. For example, the auxiliary recording layer 22 is formed by sputtering with use of a sputtering target containing oxide, or by reactive sputtering where oxygen is incorporated at a partial pressure of 0.5 to 3%.

Thus, the magnetic disk according to the present invention is provided with the auxiliary recording layer containing 0.1 to 3 mol % of oxygen on the magnetic recording layer, thereby improving uniformity of the grain boundary among magnetic particles in the auxiliary recording layer. As a result, uniformity in magnetic continuity is also improved, and consequently noise can be reduced even in a magnetic disk comprising the magnetic recording layer, which has a granular structure and a recording capacity of 250 G or more bits per square inch.

Embodiment 2

In Embodiment 2, a magnetic disk configuration different from that according to Embodiment 1 will be described.

In general, important for improving a recording density in a magnetic disk are improvements in static magnetic characteristics such as the coercive force Hc and reverse magnetic domain nucleus forming magnetic field Hn mentioned above, and in electromagnetic conversion characteristics such as overwrite characteristics (OW characteristics), SNR (Signal Noise Ratio), and narrowing of track width. In particular, the auxiliary recording layer may be disposed above or below the magnetic recording layer in order to improve OW characteristics. The auxiliary recording layer is a magnetic layer almost magnetically continuous in the in-plane direction on the main surface of the disk substrate, and improves the OW characteristics by exerting a magnetic interaction on the magnetic recording layer to raise the reverse magnetic domain nucleus forming magnetic field Hn.

However, with the auxiliary recording layer disposed, so-called “blurred writing” is caused and the track width is increased in exchange for the improvement in the OW characteristics. Moreover, the blurred writing has an influence on adjacent recording bits and tracks, deteriorating the signal quality of the adjacent tracks. In other words, the auxiliary recording layer is originally intended to improve a surface recording density by lowering coercive force Hc and improving SNR to improve a linear recording density, but the influence of the existence of the auxiliary recording layer on the adjacent tracks reduces track density and accordingly lowers surface recording density. On the other hand, if the thickness of the auxiliary recording layer is made thinner in order to avoid the blurred writing, then recording itself will be difficult (due to poorer OW characteristics), and more noise will be caused.

Therefore, it is necessary to deposit the auxiliary recording layer with a suitable film thickness. However, the behavior of the auxiliary recording layer is very sensitive to its film thickness: namely, if there is any difference in film thickness from an ideal value, blurred writing will increase or the OW characteristics will deteriorate. Thus, in the auxiliary recording layer, the blurred writing and the OW characteristic are in a trade-off relation, and are difficult to stably balance as desired.

An object of Embodiment 2 is to provide a magnetic disk which can improve recording density by achieving compatibility between a track width and SNR, namely by maintaining the film thickness of the auxiliary recording layer to keep OW characteristics in a good state while narrowing a track width and improving SNR.

In order to solve the above-mentioned problems, the inventor earnestly considered and conceived that the auxiliary recording layer is formed so as to have a two-layer structure, in which one layer at a closer side to the magnetic recording layer has a granular structure and acts as a pin layer (magnetization direction fixing layer) for another layer at a far side. The structure is described below with reference to the drawings.

[Perpendicular Magnetic Recording Medium]

FIG. 3 illustrates the configuration of a perpendicular magnetic recording medium 150 according to Embodiment 2. The perpendicular magnetic recording medium 150 shown in FIG. 3 is composed of a disk substrate 110, an adhesion layer (adhesive layer) 112, a first soft magnetic layer 114 a, a spacer layer 114 b, a second soft magnetic layer 114 c, a primary underlayer 116 (non-magnetic layer), a first underlayer 118 a, a second underlayer 118 b, a non-magnetic granular layer 120, a lower recording layer 122 a, an interposed layer 122 b, a first main recording layer 122 c, a second main recording layer 122 d, a separation layer 124, a granular auxiliary recording layer 126 a, a non-granular auxiliary recording layer 126 b, a medium protective layer 128, and a lubricant layer 130. The first soft magnetic layer 114 a, the spacer layer 114 b, and the second soft magnetic layer 114 c together constitutes a soft magnetic layer 114. The first underlayer 118 a and the second underlayer 118 b together constitutes an underlayer 118. The lower recording layer 122 a, the interposed layer 122 b, the first main recording layer 122 c, and the second main recording layer 122 d together constitutes a magnetic recording layer 122. The granular auxiliary recording layer 126 a and the non-granular auxiliary recording layer 126 b together constitutes an auxiliary recording layer 126.

As the disk substrate 110, a glass disk can be used which is obtained by molding amorphous aluminosilicate glass in a disk shape by direct-pressing. Note that there is no particular restriction on the type, size, thickness, and others of the glass disk. Examples of a material of the glass disk include, for example, aluminosilicate glass, soda lime glass, soda aluminosilicate glass, aluminoborosilicate glass, borosilicate glass, quartz glass, chain silicate glass, or glass ceramic such as crystallized glass. The glass disk is sequentially ground, polished, and chemically strengthened to obtain a smooth non-magnetic disk substrate 110 composed of chemically strengthened glass disk.

On the substrate 110, films from the adhesion layer 112 to the auxiliary recording layer 126 are sequentially deposited by a DC magnetron sputtering method, and the medium protective layer 128 can be deposited by a CVD method. Then, the lubricant layer 130 can be deposited by a dip coating method. Note that it is also preferable to use an in-line deposition method because of its high productivity. The structure of individual layers will be described below.

The adhesion layer 112 is formed in contact with the disk substrate 110, and has functions of increasing peel strength between the soft magnetic layer 130 and the disk substrate 110 formed thereon, and of fining and uniforming crystal grains of each layer deposited on the soft magnetic layer 114. If the disk substrate 110 is composed of amorphous glass, the adhesive layer 112 is preferably an amorphous (non-crystalline) alloy film so as to be compatible with the amorphous glass surface.

The adhesion layer 112 can be selected from, for example, a CrTi-based amorphous layer, a CoW-based amorphous layer, a CrW-based amorphous layer, a CrTa-based amorphous layer, or a CrNb-based amorphous layer. The adhesion layer 112 may be a single layer composed of a single material, or may be formed by laminating two or more layers. For example, a CoW or CrW layer may be formed on a CrTi layer. Moreover, these adhesive layers 112 are preferably made by sputtering with use of a material containing carbon dioxide, carbon monoxide, nitrogen or oxygen, or by exposing the surface layer to these gases.

The soft magnetic layer 114 is a layer for forming a magnetic path temporarily at the time of recording in order to allow a magnetic flux to pass through the record layer perpendicularly in a perpendicular magnetic recording system. The soft magnetic layer 114 may be configured so that the non-magnetic spacer layer 114 b is interposed between the first soft magnetic layer 114 a and the second soft magnetic layer 114 c to cause AFC (Antiferromagnetic exchange coupling). Thereby, the magnetizing direction of the soft magnetic layer 114 can be aligned along the magnetic path (magnetic circuit) with high accuracy, and the perpendicular components of the magnetizing direction can be extremely reduced, so that less noise can be caused from the soft magnetic layer 114. For example, a cobalt-based alloy such as CoTaZr, a Co—Fe-based alloy such as CoCrFeB or CoFeTaZr, or a Ni—Fe-based alloy such as a [Ni—Fe/Sn]_(n) multilayer structure can be used to compose the first soft magnetic layer 114 a and the second soft magnetic layer 114 c.

The primary underlayer (orientation control layer) 116 is a non-magnetic layer, or namely a non-magnetic alloy layer, and has effects of protecting the soft magnetic layer 114 and of promoting the alignment of the orientation of crystal grains in the underlayer 118. A material of the primary underlayer 116 can be specifically selected from Ni, Cu, Pt, Pd, Zr, Ta, Hf, and Nb. Further, the material may be an alloy based on any of the metals and including any one or more of additional elements of Ti, V, Ta, Cr, Mo, and W. For example, NiW, NiCr, a NiTa alloy, a CuW alloy, and a CuCr alloy can be selected suitably. Moreover, the primary underlayer layer may be formed of two or more layers.

This improves the roughness of each boundary surface between two or more layers formed on the soft magnetic layer 114, and thereby improves the crystal orientation of these layers. Therefore, SNR and recording density can be improved.

The underlayer 118 has an hcp structure and an effect of growing Co crystals of an hcp structure in the magnetic recording layer 122 into those of a granular structure. Therefore, as the crystal orientation of the underlayer 118 is higher, namely as the crystal (0001) surface of the underlayer 118 is more parallel to the main surface of the disk substrate 110, the orientation of the magnetic recording layer 122 can be improved. In addition, in order to give separativeness, the underlayer 118 may be formed of a lower layer to which a lower Ar pressure is applied at the time of deposition and an upper layer to which a higher Ar pressure is applied thereat. A material of the underlayer 118 is typically Ru, but can be also selected from Re, Pt, RuCr, or RuCo. Ru has an hcp structure and a similar crystal interatomic distance to that of Co, and can therefore satisfactorily orient the Co-based magnetic recording layer 122. Any oxide may be also added.

If the underlayer 118 is made of Ru, the underlayer can be formed of two layers composed of Ru by changing a gas pressure at the time of sputtering. Specifically, when the first underlayer 118 a at a lower layer side is formed, Ar gas pressure is made the specified pressure, namely a lower pressure, while when the second underlayer 118 b at a upper layer side is formed, Ar gas pressure is made higher than that when the first underlayer 118 a at a lower layer side is formed, namely a higher pressure. Thereby, the crystal orientation of the magnetic recording layer 122 can be improved by the first underlayer 118 a, and the grain diameter of the magnetic particles in the magnetic recording layer 122 can be decreased by the second underlayer 118 b.

Moreover, when the gas pressure is made higher, the mean free path of plasma ions to be sputtered becomes shorter, and accordingly the depositing speed becomes slower and a film rougher. As a result, separation and micronization of the crystal grains of Ru can be promoted, and the crystal grains of Co can be micronized.

Furthermore, minute amounts of oxygen may be incorporated into Ru of the underlayer 118. Thereby, separation and micronization of the crystal grains of Ru can be further promoted, and the magnetic recording layer 122 can be further isolated and micronized. Therefore, according to Embodiment 2, oxygen is incorporated into the second underlayer, which is one of two layers constituting the underlayer 118 and deposited just below the magnetic recording layer. In other words, the second underlayer is composed of RuO, so that the above-mentioned advantages can be acquired the most effectively. Note that, although oxygen may be incorporated by reactive sputtering, a target containing oxygen is preferably used at the time of sputtering deposition.

The non-magnetic granular layer 120 is a non-magnetic layer having a granular structure. By forming the non-magnetic granular layer 120 on the hcp crystal structure of the underlayer 118 and growing the granular layer of the lower recording layer 122 a (namely, the whole of the magnetic recording layer 122) thereon, the magnetic granular layer can be separated from the stage of initial growth (initial rise). Thereby, isolation of magnetic particles in the magnetic recording layer 122 can be promoted. The non-magnetic granular layer 120 can be composed to have a granular structure, by precipitating non-magnetic substances among non-magnetic crystal grains composed of a Co-based alloy to form a grain boundary.

According to Embodiment 2, CoCr—SiO₂ is used for such a non-magnetic granular layer 120. Thereby, SiO₂ (non-magnetic substance) precipitates between Co-based alloys (non-magnetic crystal grains) to form a grain boundary, so that the non-magnetic granular layer 120 can have a granular structure. Note that CoCr—SiO₂ is merely an example and is not intended to be limiting. Besides, CoCrRu—SiO₂ can be suitably used, and furthermore, Rh (rhodium), Pd (palladium), Ag (silver), Os (osmium), Ir (iridium), and Au (gold) can be also used instead of Ru. Note that a non-magnetic substance means a substance which can form a grain boundary portion (grain boundary region) around magnetic particles so as to suppress or block exchange interaction between the magnetic particles (magnetic grains), and also means a non-magnetic substance which does not form a solid solution with cobalt (Co). For example, silicon oxide (SiOx), chromium (Cr), chromium oxide (Cr₂O₃), titanium oxide (TiO₂), zirconium oxide (ZrO₂), and tantalum oxide (Ta₂O₅) can be mentioned.

Note that Embodiment 2 has a configuration with the non-magnetic granular layer 120 formed on the underlayer 118 (the second underlayer 118 b), but is not intended to limit to the configuration, and that the perpendicular magnetic recording medium 100 may be also configured without forming the non-magnetic granular layer 120.

The magnetic recording layer 122 has a columnar granular structure which is formed by precipitating a non-magnetic substance around the magnetic particles in a hard-magnetic material selected from a Co-based alloy, a Fe-based alloy, and a Ni-based alloy to form the grain boundary (granular magnetic recording layer). By providing the non-magnetic granular layer 120, these magnetic particles can epitaxially grow continuously from the granular structure thereof. According to Embodiment 2, the magnetic recording layer 122 is composed of the lower recording layer 122 a, the interposed layer 122 b, the first main recording layer 122C, and the second main recording layer 122 d. Thereby, small crystal grains in the first main recording layer 122 c and the second main recording layer 122 d grow continuously from the crystal particles (magnetic particles) in the lower recording layer 122 a, so that the main recording layer can be micronized and SNR can be improved.

According to Embodiment 2, CoCrPt—Cr₂O₅—SiO₂ is used for the lower recording layer 122 a. CoCrPt—Cr₂O₅—SiO₂ forms a granular structure where Cr₂O₅ and SiO₂ (oxides), which are non-magnetic substances, precipitate around the magnetic particles (grains) composed of CoCrPt to form a grain boundary, and where the magnetic particles grow in a columnar shape. The magnetic particles epitaxially grew continuously from the granular structure of the non-magnetic granular layer 120.

The interposed layer 122 b is a non-magnetic thin film, and is interposed between the lower recording layer 122 a and the first main recording layer 122 c to separate the magnetic continuity therebetween. Here, with the thickness of the interposed layer 122 b being made the specified thickness (0.2 to 0.9 nm), antiferromagnetic exchange coupling (AFC) may occur between the lower recording layer 122 a and the first main recording layer 122 c. Thereby, the layers at the upper and lower sides of the interposed layer 122 b attract each other due to magnetization and act to mutually fix their magnetization directions, so that fluctuation of a magnetization axis can be reduced, and less noise can be caused.

The interposed layer 122 b is preferably composed of Ru or a Ru compound. The reason for this is that Ru has a similar interatomic distance to that of Co constituting magnetic particles, and therefore hardly impedes epitaxial growth of the crystal grains of Co even if interposed into the magnetic recording layer 122. Moreover, the epitaxial growth is hardly impeded because of extremely thin thickness of the interposed layer 122 b.

Here, without the interposed layer 122 b, the lower recording layer 122 a would be a magnet which is continuous with the first main recording layer 122 c and the second main recording layer 122 d. However, since divided by the interposed layer 122 b, each of those layers becomes an individual short magnet. Further, by making the thickness of the lower recording layer 122 a thinner, the aspect ratio of granular magnetic particles shrinks (in the perpendicular magnetic recording medium, the film thickness direction is equal to the longitudinal direction of a easy magnetization axis), thereby strengthening a demagnetizing field which generates inside the magnet. Therefore, although having hard magnetism, the lower recording layer 122 a emits a smaller magnetic moment outside, and is hardly captured by a magnetic recording head. In other words, a magnetic recording layer with high coercive force and less noise can be obtained by adjusting the thickness of the lower recording layer 122 a to set a magnetic moment (magnetic strength) to such a degree that a magnetic flux hardly reaches a magnetic recording head and that a magnetic interaction can be given to the first main recording layer 122 c.

According to Embodiment 2, CoCrPt—SiO₂—TiO₂ is used for the first main recording layer 122 c. Thereby, the first main recording layer 122 c also formed a granular structure where SiO₂ and TiO₂ (composite oxides), which are non-magnetic substances, precipitate around the magnetic particles (grains) composed of CoCrPt to form a grain boundary, and where the magnetic particles grow in a columnar shape.

Moreover, according to Embodiment 2, although the second main recording layer 122 d is continuous with the first main recording layer 122 c, their compositions and film thickness are different. CoCrPt—SiO₂—TiO₂—Co₃O₄ is used for the second main recording layer 122 d. Thereby, the second main recording layer 122 d also formed a granular structure where SiO₂, TiO₂, and Co₃O₄ (composite oxides), which are non-magnetic substances, precipitate around the magnetic particles (grains) composed of CoCrPt to form a grain boundary, and where the magnetic particles grow in a columnar shape.

As described above, according to Embodiment 2, the second main recording layer 122 d is configured to contain more oxides than the first main recording layer 122 c, so that separation of crystal grains can be promoted in stages from the first main recording layer 122 c to the second main recording layer 122 d.

Moreover, the second main recording layer 122 d is made to contain Co oxides as described above. If an oxide such as SiO₂ or TiO₂ is incorporated, oxygen will be depleted, and a Si or Ti ion will be mixed into magnetic particles, thereby disturbing crystal orientation and decreasing the coercive force Hc. Therefore, when a Co oxide is incorporated, the Co oxide can act as an oxygen carrier for making up for such oxygen depletion. As the Co oxide, Co₃O₄ is mentioned, but CoO may be used.

Co oxide has larger Gibss free energy ΔG(delta G) than SiO₂ and TiO₂, and facilitates separation between Co ions and oxygen ions. Therefore, oxygen preferentially separates from Co oxide, and compensates oxygen depletion caused in SiO₂ or TiO₂ to make Si or Ti ions into oxides and precipitate the oxides on a grain boundary. This prevents foreign particles such as Si and Ti from being mixing into magnetic particles and disturbing the crystallinity of the magnetic particles. Any surplus Co ions could be contained in the magnetic particles, but would not impair magnetic characteristics because magnetic particles themselves are Co alloys. Consequently, the crystallinity and crystal orientation of the magnetic particles can be improved, and coercive force Hc can be increased. Moreover, there is another advantage that the overwrite characteristics are also improved because the saturation magnetization Ms is improved.

However, there is a problem that SNR decreases when Co oxide is mixed in the magnetic recording layer. Therefore, by providing the first main recording layer 122 c containing no Co oxide as described above, high SNR can be secured in the first main recording layer 122 c, while higher coercive force Hc and over write characteristics can be obtained in the second main recording layer 122 d. Note that the film thickness of the second main recording layer 122 d is preferably thicker than that of the first main recording layer 122 c, and, as a suitable example, the film thickness of the first main recording layer 122 c can be 4 nm while that of the second main recording layer 122 d can be 6 nm.

Note that the substances used for the lower recording layer 122 a, the first main recording layer 122 c, and the second main recording layer 122 d are merely examples, and are not intended to be limiting. Examples of a non-magnetic substance for forming a grain boundary include, for example, oxides such as silicon oxide (SiOx), chromium (Cr), chrome oxide (CrxOy), titanium oxide (TiO₂), zirconium oxide (ZrO₂), tantalum oxide (Ta₂O₅), iron oxide (Fe₂O₃), and boron oxide (B₂O₃). Moreover, nitride such as BN and carbide such as B₄C₃ can be also suitably used.

Furthermore, according to Embodiment 2, two types of non-magnetic substances (oxides) are used for the lower recording layer 122 a and the first main recording layer 122 c while three types of those for the second main recording layer 122 d, but they are not intended to be limiting. For example, one type of non-magnetic substance or a combination of two or more types of non-magnetic substances may be used for any or all of the layers from the lower recording layer 122 a to the second main recording layer 122 d. Although the type of non-magnetic substances contained therein is not limited, especially SiO₂ and TiO₂ are preferably incorporated as described in Embodiment 2. Therefore, unlike Embodiment 2, if only one layer constitutes the magnetic recording layer from the lower recording layer 122 a to the second main recording layer 122 d (if the interposed layer 122 b is not provided), the magnetic recording layer preferably comprises CoCrPt—SiO₂—TiO₂.

The separation layer 124 is a non-magnetic layer interposed between the magnetic recording layer 122 (the second main recording layer 122 d) and the auxiliary recording layer 126. By providing the separation layer, the strength of ferromagnetic exchange coupling between the magnetic recording layer and the auxiliary recording layer can be controlled. The film thickness of the separation layer is preferably within the range of 0.1 to 1.0 nm.

Moreover, according to Embodiment 2, the separation layer 124 can be composed of a thin film containing Ru, a Ru compound, Ru and oxygen, or Ru and an oxide. This also reduces noise resulting from the auxiliary recording layer 126. The reason for this is considered that, when the separation layer 124 is deposited, oxygen contained in the separation layer 124 precipitates on the oxides in the magnetic recording layer 122 and Ru precipitates on the magnetic particles, so that the crystal structure of Co in the magnetic recording layer 122 can be succeeded to Co of the auxiliary recording layer 126.

Various materials can be used as oxides to be incorporated into Ru of the separation layer 124, but especially alloys and oxides of W, Ti and Ru can be used to improve the electromagnetic conversion characteristic (SNR). For example, the separation layer 124 may be made of RuCr, RuCo, RuO, RuWO₃, or RuTiO₂, or any material obtained by incorporating an oxide into RuCr or RuCo. Especially, RuCr, RuCo, and WO₃ can have a higher effect.

As for RuWo₃, the oxygen incorporated into Ru dissociates during sputtering, and the dissociated oxygen also shows the effect by oxygenation. In other words, RuWo₃ is preferable for that reason that the use of Wo₃ can provide both effects by oxygenation and oxide addition. Another reason may be because of higher material affinity at the time of laminating since oxides are incorporated in the layers above and below the separation layer according to Embodiment 2. Other examples of oxides include oxides such as silicon oxide (SiOx), chromium (Cr), chrome oxide (CrxOy), titanium oxide (TiO₂), zirconium oxide (ZrO₂), tantalum oxide (Ta₂O₅), iron oxide (Fe₂O₃), and boron oxide (B₂O₃). Moreover, nitride such as BN and carbide such as B₄C₃ can be also suitably used. Note that RuCr and RuCo is considered to show excellent characteristics because of higher affinity since Cr and Co are contained in the layers above and below the separation layer.

According to Embodiment 2, the auxiliary recording layer 126 is composed of two layers of the granular auxiliary recording layer 126 a and the non-granular auxiliary recording layer 126 b. First, the non-granular auxiliary recording layer 126 b will be described. The non-granular auxiliary recording layer 126 b is a magnetic layer almost magnetically continuous in the in-plane direction of the main surface of the substrate. The non-granular auxiliary recording layer 126 b needs to be adjacent or close to the magnetic recording layer 122 so as to have a magnetic interaction on the magnetic recording layer 122. The non-granular auxiliary recording layer 126 b can be composed of, for example, CoCrPt, CoCrPtB, or any substance obtained by incorporating minute amounts of oxides into them. An object of the non-granular auxiliary recording layer 126 b is to adjust a reverse magnetic domain nucleus forming magnetic field Hn and a coercive force Hc and to thereby improve thermal fluctuation resistance, OW characteristics, and SNR. In order to attain this object, the non-granular auxiliary recording layer 126 b preferably has high perpendicular magnetic anisotropy Ku and saturation magnetization Ms.

Note that “magnetically continuous” means that magnetism continues without interruption. “Almost continuous” means that the non-granular auxiliary recording layer 126 b may be not necessarily a single magnet when observed as a whole and may have partially discontinuous magnetism due to the grain boundary of magnetic particles. In the grain boundary, not only crystals may be discontinuous, but also Cr may precipitates, or may be caused to precipitate by incorporating minute amounts of oxides thereinto. However, even if the grain boundary containing oxide is formed in the non-granular auxiliary recording layer 126 b, the area of the grain boundary is preferably smaller (less content of oxide) than that in the magnetic recording layer 122. Although the function and effect of the non-granular auxiliary recording layer 126 b are not necessarily clear, it is considered that the non-granular auxiliary recording layer 126 b has a magnetic interaction (makes exchange coupling) with the granular magnetic particles in the magnetic recording layer 122, thereby adjusting Hn and Hc to improve thermal fluctuation resistance and SNR. It is also considered that a crystal grain which is linked to a granular magnetic particle (a crystal grain having a magnetic interaction therewith) has a larger cross sectional area than the granular magnetic particle, thereby receiving more magnetic fluxes from a magnetic head and causing magnetization reversal more easily, consequently leading to the improvement in the whole OW characteristics.

FIG. 4 illustrates a layer structure from the main recording layer to the auxiliary recording layer. According to Embodiment 2, the granular auxiliary recording layer 126 a, which has higher coercive force than the non-granular auxiliary recording layer 126 b and has a granular structure, is provided below the non-granular auxiliary recording layer 126 b. In FIG. 4, a shaded area shows granular magnetic particles. The granular auxiliary recording layer 126 a is magnetically separated from the second main recording layer 122 d by the separation layer 124, and can reverse its magnetization direction independently from the second main recording layer 122 d. Then, the granular auxiliary recording layer 126 a exerts a magnetic interaction on the non-granular auxiliary recording layer 126 b, thereby acting to make it hard to reverse the magnetization direction of the auxiliary recording layer 126. Note that the thickness of the separation layer 124 deposited is so extremely thin (approximately 0.7 nm) that the granular auxiliary recording layer 126 a grows its crystals in succession to the granular structure of the second main recording layer 122 d.

According to the above-mentioned configuration, the granular auxiliary recording layer 126 a having higher coercive force acts as a pin layer of the non-granular auxiliary recording layer 126 b. Therefore, while more blurred writing are generally caused when a thicker auxiliary recording layer is used, a track width can be made narrower (blurred writing can be reduced) and SNR can be improved even if a thicker auxiliary recording layer is provided. Thus, compatibility between a track width and SNR can be achieved.

The above-mentioned granular auxiliary recording layer 126 a has lower at % of Cr and higher at % of CoPt than the first main recording layer 122 c and the second main recording layer 122 d. The reason is that, according to this composition, the granular auxiliary recording layer 126 a has higher coercive force than the first main recording layer 122 c and the second main recording layers 122 d, and ideally acts as a pin layer of the non-granular auxiliary recording layer 126 b.

According to Embodiment 2, the difference (A-B) between the Cr concentration (A) of the magnetic recording layer 122 and the Cr concentration (B) of the granular auxiliary recording layer 126 a is not less than 1 at % and not more than 4 at %. Compared to the first main recording layer 122 c and the second main recording layer 122 d, at % of Cr is made smaller and at % of CoPt is made larger to increase coercive force.

According to Embodiment 2, the granular auxiliary recording layer 126 a has thinner film thickness than the non-granular auxiliary recording layer 126 b. The reason for this is that, if the non-granular auxiliary recording layer 126 b is made thinner, recording itself will be impossible, therefore the thickness of the non-granular auxiliary recording layer is maintained to keep OW characteristics, while a blurred writing is prevented by the granular auxiliary recording layer which acts as a pin layer of the non-granular auxiliary recording layer 126 b. According to Embodiment 2, it is preferable that the thickness of the granular auxiliary recording layer is 0.5 to 5.0 nm, and that of the non-granular auxiliary recording layer is 4.0 to 8.0 nm.

The medium protective layer 128 can be formed by depositing carbon by a CVD method with maintaining a vacuum. The medium protective layer 128 is a layer for protecting the perpendicular magnetic recording medium 100 against impacts from a magnetic recording head. In general, as compared with carbon deposited by a sputtering method, carbon deposited by a CVD method has higher film hardness, and thereby can more effectively protect the perpendicular magnetic recording layer 100 against impacts from the magnetic recording head.

The lubricant layer 130 is deposited by coating PFPE (perfluoropolyether) by a dip-coating method. PFPE has a long-chain molecular structure and is bound to an N atom on the surface of the medium protective layer 128 with high affinity. This action of the lubricant layer 130 prevents damage or loss to the medium protective layer 128, even if the magnetic recording head makes contact with the surface of the perpendicular magnetic recording medium 100.

The examples, which were implemented to make the effects of the present invention clear, will be described bellow. Note that, in the following description, Examples 1 and 2 correspond to Embodiments 1 and 2, respectively.

Example 1 Example 1-1

An aluminosilicate-based amorphous chemically strengthened glass substrate with a smooth surface was used as a non-magnetic substrate. After being washed, the glass substrate was placed into a DC magnetron sputtering device to deposit a Cr-50Ti thin film of 10 nm in thickness (adhesive layer 12), a 92(40Fe-60Co)-3Ta-5Zr thin film of 24 nm in thickness (first soft magnetic layer), a Ru thin film of 0.5 nm in thickness (spacer layer), a 92(40Fe-60Co)-3Ta-5Zr thin film of 24 nm in thickness (second soft magnetic layer 14), a 95Ni-5W thin film of 5 nm in thickness (orientation control layer 16), a Ru thin film of 20 nm in thickness (underlayer 18), a 90(Co-14Cr-16Pt)-10(SiO₂) thin film of 12 nm in thickness (magnetic recording layer 20), and an oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness (auxiliary recording layer 22), and then to deposit a medium protective layer 24 composed of carbon and having a thickness of 5 nm. As for the Ar gas pressure at the time of sputtering of each metallic film except for the protective layer, the pressure is set to 0.6 Pa for the first half (10 nm in thickness) of the underlayer 18, 5.0 Pa for the second half (10 nm in thickness) of the underlayer 18, 4.0 Pa for the magnetic recording layer 20, and 0.6 Pa for other layers. Then, the glass substrate was removed from the DC magnetron sputtering device, and was washed before being applied with a lubricant (PFPE) by a dip-coating method, and then was baked to form a lubricant layer 26 of 1 nm in thickness. Thus produced was a magnetic disk of Example 1-1 for a recording capacity of 250 G bits per square inch. The auxiliary recording layer 22 was deposited by reactive sputtering where oxygen gas was incorporated into treatment gas (Ar gas) at a partial pressure of 3%, and then the oxygen content was confirmed to be 3 mol %.

Example 1-2

A magnetic disk of Example 1-2 was produced in the same manner as in Example 1-1, except that instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 98(Co-20Cr-19Pt-3B)-2(CuO) target.

Example 1-3

A magnetic disk of Example 1-3 was produced in the same manner as in Example 1-1, except that instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 98(Co-20Cr-19Pt-3B)-2(CoO) target.

Example 1-4

A magnetic disk of Example 1-4 was produced in the same manner as in Example 1-1, except that instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 98(Co-20Cr-19Pt-3B)-2(SiO₂) target.

Example 1-5

A magnetic disk of Example 1-5 was produced in the same manner as in Example 1-1, except that instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 98(Co-20Cr-19Pt-3B)-2(TiO₂) target.

Example 1-6

A magnetic disk of Example 1-6 was produced in the same manner as in Example 1-1, except that instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 94(Co-20Cr-19Pt-3B)-6(CuO) target.

Comparative Example 1-1

A magnetic disk of Comparative Example 1-1 was produced in the same manner as in Example 1-1, except that instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 was formed which is composed of a Co-20Cr-19Pt-3B thin film of 7 nm in thickness.

Comparative Example 1-2

A magnetic disk of Comparative Example 1-1 was produced in the same manner as in Example 1-1, except that instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 was formed which is composed of a 92(Co-20Cr-19Pt-3B)-8(Cuo) thin film of 7 nm in thickness.

The magnetic disks of Examples 1-1 to 1-6 and Comparative Examples 1-1 and 1-2 were investigated for track width (magnetic write width (MWW)) and bit error rate (digit). The results are shown in Table 1 below. Note that the bit error rate was calculated by the following formula (I), after 107 pieces of known random data were recorded at 1300 kFCI (overwrite characteristics) using a spin stand and the number of reading errors was counted. In addition, the magnetic write width was calculated from the track profile using the spin stand.

bER=log(number of errors/number of data pieces)  Formula (1)

TABLE 1 Oxygen Track Bit content width error rate Auxiliary recording layer Process (mol %) (nm) (digit) Example 1-1 Co—20Cr—19Pt—3B Reactive sputtering 3 108 −6.1 Example 1-2 98(Co—20Cr—19Pt—3B)—2(CuO) Sputtering 1 106 −6.5 Example 1-3 98(Co—20Cr—19Pt—3B)—2(CoO) Sputtering 1 106 −6.3 Example 1-4 98(Co—20Cr—19Pt—3B)—2(Si₂O) Sputtering 2 107 −5.7 Example 1-5 98(Co—20Cr—19Pt—3B)—2(Ti₂O) Sputtering 2 109 −5.8 Example 1-6 94(Co—20Cr—19Pt—3B)—6(CuO) Sputtering 3 106 −5.8 Comparative Example 1-1 Co—20Cr—19Pt—3B Sputtering 0 107 −5.2 Comparative Example 1-2 92(Co—20Cr—19Pt—3B)—8(CuO) Sputtering 4 106 −5.2

As can be seen from Table 1, the bit error rates of the magnetic disks of Examples 1-1 to 1-6 were relatively lower. The reason for this is considered that with 0.1 to 3 mol % of oxygen contained in the auxiliary recording layers, structural non-uniformity caused in the course of laminating the auxiliary recording layer was able to be reduced, and accordingly noise from the auxiliary recording layer resulting from the non-uniformity was reduced. On the other hand, the bit error rate of the magnetic disk of Comparative Example 1-1 was relatively higher. The reason for this is considered that without any oxygen contained in the auxiliary recording layer, the grain boundary portion present between magnetic particles became unstable and the film uniformity degraded, thereby noise became larger. The bit error rate of the magnetic disk of Comparative Example 1-2 was also relatively higher compared to that of the magnetic disks of Examples 1-1 to 1-6. The reason for this is considered that with more than 3 mol % (4 mol %) of oxygen contained in the auxiliary recording layer, the magnetic continuity in the in-plane direction of the magnetic disk was excessively lost, thereby the overwrite characteristics deteriorated. Note that the track widths in any Examples were within the range of ±2 nm of the values in Comparative Examples, and can be therefore considered equivalent in view of a measurement error.

Next, examples will be described where a magnetic recording layer is formed so as to contain two or more oxides.

Example 1-7

A magnetic disk of Example 1-7 was produced in the same manner as in Example 1-1, except that instead of the 90(Co-14Cr-16Pt)-10(SiO₂) thin film of 12 nm in thickness, a magnetic recording layer 20 of 12 nm in thickness was formed by sputtering with use of a 90(Co-14Cr-16Pt)-5(SiO₂)-5(TiO₂) target, and instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 98(Co-20Cr-19Pt-3B)-2(CuO) target.

Example 1-8

A magnetic disk of Example 1-8 was produced in the same manner as in Example 1-1, except that instead of the 90(Co-14Cr-16Pt)-10(SiO₂) thin film of 12 nm in thickness, a magnetic recording layer 20 of 12 nm in thickness was formed by sputtering with use of a 89(Co-14Cr-16Pt)-5(SiO₂)-5(TiO₂)-1(Co₃O₄) target, and instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 98(Co-20Cr-19Pt-3B)-2(CuO) target.

Example 1-9

A magnetic disk of Example 1-9 was produced in the same manner as in Example 1-1, except that instead of the 90(Co-14Cr-16Pt)-10(SiO₂) thin film of 12 nm in thickness, a magnetic recording layer 20 of 12 nm in thickness was formed by sputtering with use of a 90(Co-14Cr-16Pt)-5(SiO₂)-5(TiO₂) target, and instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 98(Co-20Cr-19Pt-3B)-2(CoO) target.

Example 1-10

A magnetic disk of Example 1-10 was produced in the same manner as in Example 1-1, except that instead of the 90(Co-14Cr-16Pt)-10(SiO₂) thin film of 12 nm in thickness, a magnetic recording layer 20 of 12 nm in thickness was formed by sputtering with use of a 89(Co-14Cr-16Pt)-5(SiO₂)-5(TiO₂)-1(Co₃O₄) target, and instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 98(Co-20Cr-19Pt-3B)-2(CoO) target.

Example 1-11

A magnetic disk of Example 1-11 was produced in the same manner as in Example 1-1, except that instead of the 90(Co-14Cr-16Pt)-10(SiO₂) thin film of 12 nm in thickness, a magnetic recording layer 20 of 12 nm in thickness was formed by sputtering with use of a 90(Co-14Cr-16Pt)-10(TiO₂) target, and instead of the oxygen-containing Co-20Cr-19Pt-3B thin film of 7 nm in thickness, an auxiliary recording layer 22 of 7 nm in thickness was formed by sputtering with use of a 98(Co-20Cr-19Pt-3B)-2(CuO) target.

The magnetic disks of Examples 1-7 to 1-11 were investigated for magnetic write width (MWW) and bit error rate (digit). The results are shown in Table 2 below. Note that the bit error rate was calculated by the above-mentioned formula (I), after 107 pieces of known random data were recorded at 1300 kFCI (overwrite characteristics) using a spin stand and the number of reading errors was counted. In addition, the magnetic write width was calculated from the track profile using the spin stand.

TABLE 2 Oxygen Track Bit content width error rate Magnetic recording layer Auxiliary recording layer (mol %) (nm) (digit) Example 1-7 90(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂) 98(Co—20Cr—19Pt—3B)—2(CuO) 1 104 −6.8 Example 1-8 89(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂)—1(Co₃O₄) 98(Co—20Cr—19Pt—3B)—2(CuO) 1 101 −6.9 Example 1-9 90(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂) 98(Co—20Cr—19Pt—3B)—2(CuO) 1 105 −6.6 Example 1-10 89(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂)—1(Co₃O₄) 98(Co—20Cr—19Pt—3B)—2(CuO) 1 101 −6.7 Example 1-11 90(Co—14Cr—16Pt)—10(TiO₂) 98(Co—20Cr—19Pt—3B)—2(CuO) 1 106 −6.7

According to Table 2, it was confirmed that the magnetic recording layer having two or more oxides improved the characteristics better. The reason for this is as follows. In the magnetic layer with a granular structure, which is deposited by sputtering, such as 90(Co-14Cr-16Pt)-10(SiO₂), oxygen is depleted, and consequently Si is incorporated into the inside of magnetic particles (CCP), deteriorating magnetic anisotropy energy, but oxygen depletion can be compensated by mixing oxides thereinto. In addition, Example 1-8 shows the best characteristics. The reason for this is considered that Co oxide has higher Gibbs energy (is unstable as an oxide), so that Co and O can be easily separated, and that the separated Co is incorporated into the inside of a magnetic layer to allow O to compensate oxygen depletion in Si or Ti. Here, Co₃O₄ was used, but CoO may be used.

Next, examples will be described where a separation layer is formed between the magnetic recording layer and the auxiliary recording layer.

Example 1-12

A magnetic disk of Example 1-12 was produced in the same manner as in Example 1-8, except that a separation layer was formed between the magnetic recording layer and the auxiliary recording layer. The separation layer was formed of a Ru thin film of 0.3 nm in thickness by sputtering at an Ar gas pressure of 0.6 Pa.

Example 1-13

A magnetic disk of Example 1-13 was produced in the same manner as in Example 1-8, except that a separation layer was formed between the magnetic recording layer and the auxiliary recording layer. The separation layer was formed of a Ru-10(WO₃) thin film of 0.5 nm in thickness by sputtering at an Ar gas pressure of 0.6 Pa.

Example 1-14

A magnetic disk of Example 1-14 was produced in the same manner as in Example 1-8, except that a separation layer was formed between the magnetic recording layer and the auxiliary recording layer. The separation layer was formed of a Ru-50Co thin film of 0.4 nm in thickness by sputtering at an Ar gas pressure of 0.6 Pa.

The magnetic disks of Examples 1-12 to 1-14 were investigated for magnetic write width (MWW) and bit error rate (digit). The results are shown in Table 3 below.

TABLE 3 Film Track Bit thickness width error rate Separation layer (nm) (nm) (digit) Example 1-8 None 0 101 −6.9 Example 1-12 Ru 0.3 98 −7.2 Example 1-13 Ru—10(WO₃) 0.5 98 −7.4 Example 1-14 Ru—50Co 0.4 97 −7.5

According to Table 3, it was confirmed that the characteristics were improved by interposing the separation layer between the magnetic recording layer and the auxiliary recording layer.

Next, examples will be described where a magnetic recording layer is formed of two or more layers.

Example 1-15

A magnetic disk of Example 1-15 was produced in the same manner as in Example 1-12, except that a magnetic disk was configured so as to have a laminated structure (three-layered structure). The laminated structure of the magnetic recording layer was deposited in three stages by sputtering with use of an 89(Co-14Cr-16Pt)-5(SiO₂)-5(TiO₂)-1(Co₃O₄) target so as to have a total thickness of 12 nm.

Example 1-16

A magnetic disk of Example 1-16 was produced in the same manner as in Example 1-12, except that a magnetic disk was configured so as to have a laminated structure (two-layered structure). The laminated structure of the magnetic recording layer was deposited in two stages by sputtering with use of an 89(Co-14Cr-16Pt)-5(SiO₂)-5(TiO₂)-1(Co₃O₄) target so as to have a total thickness of 12 nm. The two-stage deposition may be performed by using different chambers, or by forming a film with a specified film thickness, removing the film from a chamber once, and then putting it into the chamber again.

The magnetic disks of Examples 1-15 and 1-16 were investigated for magnetic write width (MWW) and bit error rate (digit). The results are shown in Table 4 below.

TABLE 4 Magnetic recording layer First layer Second layer Example 1-12 89(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂)—1(Co₃O₄) — Example 1-15 89(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂)—1(Co₃O₄) 89(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂)—1(Co₃O₄) Example 1-16 89(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂)—1(Co₃O₄) 89(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂)—1(Co₃O₄) Magnetic recording layer Track width Bit error rate Third layer (nm) (digit) Example 1-12 — 98 −7.2 Example 1-15 89(Co—14Cr—16Pt)—5(SiO₂)—5(TiO₂)—1(Co₃O₄) 95 −7.6 Example 1-16 — 97 −7.4

According to Table 4, it was confirmed that the characteristics were improved by providing a magnetic recording layer with a laminated structure. The reason for this is considered as follows. Magnetic particles will be gradually enlarged if a magnetic layer is formed by a single deposition (refer to FIG. 6). However, by performing a deposition in two or more stages to obtain a laminated structure, the enlargement of magnetic particles was prevented and the diameters of the particles in the layers from a lower layer to an upper layer were able to be made uniform. As a result, the magnetic coupling between the magnetic particles in the magnetic recording layer 20 became uniform in the depth direction, so that a medium closer to that of an ideal structure as shown in FIG. 2 can be obtained in synergy with the separation effect of adding oxygen to the auxiliary recording layer.

Example 2

On the disk substrate 110, films from the adhesion layer 112 to the auxiliary recording layer 126 were sequentially disposed in an Ar atmosphere by DC magnetron sputtering with use of a vacuumed film forming device. Note that an Ar gas pressure at the time of sputtering deposition was set to 0.6 Pa, unless otherwise specified. An adhesion layer 112 of 10 nm was formed using a Cr-50Ti target. As for a soft magnetic layer, a first soft magnetic layer 114 a and a second soft magnetic layer 114 c both of 20 nm were deposited using a 92(Co-40Fe)-3Ta-5Zr target, and a spacer layer 114 b of 0.7 nm was deposited using a Ru target. A primary underlayer 116 of 5 nm was deposited using a Ni-5W target. A first underlayer 118 a of 10 nm was deposited at 0.6 Pa using a Ru target. A second underlayer 118 b of 10 nm was deposited at 5.0 Pa using a Ru target. A non-magnetic granular layer 120 of 1 nm was deposited at 4 Pa using an 88(Co-40Cr)-12(SiO₂) target. A lower recording layer 122 a of 2.0 nm was formed at 4 Pa using a (Co-12Cr-16Pt)-2.5(Cr₂O₅)-2.5 (SiO₂) target. An interposed layer 122 b of 0.4 nm was formed using a Ru target. A first main recording layer 122 c of 4 nm was formed at 4 Pa using a 90(Co-12Cr-16Pt)-5(SiO₂)-5(TiO₂) target. A second main recording layer 122 d of 6 nm was formed at 4 Pa using a 90(Co-12Cr-16Pt)-4.5(SiO₂)-4.5(TiO₂)-1(Co₃O₄) target. A separation layer 124 of 0.5 nm was formed using a Ru-10(WO₃) target. A granular auxiliary recording layer 126 a of a specified thickness was deposited at 4 Pa using a 90(Co—Cr—Pt)-5(SiO₂)-5(TiO₂) target. The detailed composition and thickness of Co—Cr—Pt were set to the values described below. A non-granular auxiliary recording layer 126 b of 6.4 nm was formed using a Co-18Cr-15Pt-5B target. A medium protective layer 128 was deposited by a CVD method with use of C₂H₄, and a lubricant layer 130 was formed by a dip-coating method with use of PFPE.

FIG. 5 shows comparisons of track widths and SNRs between Examples 2-1 to 2-9, where a granular auxiliary recording layer 126 a of a varied film thickness is included, and Comparative Examples 2-1 and 2-2. FIGS. 5( a) and 5(b) show tabulated and plotted data, respectively.

In any of Examples and Comparative Examples, the composition and film thickness of the CoCrPt metallic phase in the granular auxiliary recording layer 126 a were changed with an at % ratio of Co:Cr:Pt of the metallic phase in the main recording layer set to 72Co-12Cr-16Pt. Note that the main recording layer and the granular auxiliary recording layer have the same number of moles of oxide.

In Examples 2-1 to 2-3 (denoted by “♦” in the graph), the at % ratio of Co:Cr:Pt of the granular auxiliary recording layer 126 a was set to 73Co-11Cr-16Pt, and the film thicknesses for the respective Examples were made into 1.4 nm, 2.6 nm, and 3.6 nm, respectively. In Examples 2-4 and 2-5 (denoted by “▪” in the graph), the at % ratio was set to 76Co-8Cr-16Pt, and the film thicknesses for the respective examples were made into 0.7 nm and 1.4 nm, respectively. In Examples 2-6 and 2-7 (denoted by “▴” in the graph), the at % ratio was set to 77Co-7Cr-16Pt, and the film thicknesses for the respective examples were made into 0.7 nm and 1.4 nm, respectively. In Examples 2-8 and 2-9 (denoted by “” in the graph), the at % ratio was set to 72Co-12Cr-16Pt, and the film thicknesses for the respective examples were made into 1.4 nm and 2.5 nm, respectively.

In addition, in Comparative Examples 2-1 and 2-2 (denoted by “∘” in the graph), no granular auxiliary recording layer 126 a was formed. In oxide-containing layers such as the granular auxiliary recording layer 126 a, the coercive force Hc is varied depending on the content of oxide and the composition of the main phase of CoCrPt. Especially, when the content of Cr, which has diamagnetism, is increased, the magnetism of Co is canceled and the coercive force Hc decreases.

Moreover, as shown in FIG. 5( a), the granular auxiliary recording layers 126 a of Examples 2-1 to 2-9 had a thinner film thickness than the non-granular auxiliary recording layers 126 b.

As shown in FIG. 5 (b), when the film thickness of each material of a granular auxiliary recording layer is made thicker, track width tends to be larger and SNR to be higher. This suggests that, under the dependence on the film thickness of the granular auxiliary recording layer, track width and SNR are in a trade-off relation, and a recording density cannot be thereby improved. On the other hand, from the viewpoint of the existence or absence of the granular auxiliary recording layer, it was found that even in consideration of the trade-off mentioned above, the characteristics were improved better in Examples 2-1 to 2-9 than in Comparative Examples 2-1 and 2-2, and that compatibility between track width and SNR were achieved.

Preferred embodiments of the present invention have been described above with reference to the attached drawings. However, needless to say, the present invention is not meant to be limited by Embodiments 1 and 2 and Examples 1 and 2. It is apparent that a person skilled in the art can conceive various modifications and alterations within the scope as described in the scope of the claims. As a matter of course, it is to be interpreted that such modifications and alterations also belong to the technical scope of the present invention.

INDUSTRIAL APPLICABILITY

The present invention can be used as a perpendicular magnetic disk mounted in an HDD of a perpendicular magnetic recording system or the like.

The present invention is based on Japanese Patent Applications No. 2008-311120 filed on Dec. 5, 2008, and No. 2009-087762 filed on Mar. 31, 2009, the entire contents of which are incorporated herein by reference. 

1. A method for manufacturing a magnetic disk comprising: a magnetic recording layer formation step of forming at least a granular magnetic recording layer on a disk substrate; and an auxiliary recording layer formation step of forming an auxiliary recording layer on the magnetic recording layer, wherein the auxiliary recording layer containing 0.1 to 3 mol % oxygen is formed in the auxiliary recording layer formation step.
 2. The method for manufacturing a magnetic disk according to claim 1, wherein the auxiliary recording layer is formed by sputtering with use of a sputtering target containing oxide in the auxiliary recording layer formation step.
 3. The method for manufacturing a magnetic disk according to claim 1, wherein the auxiliary recording layer is formed by reactive sputtering where oxygen is incorporated at a partial pressure of 0.5 to 3% in the auxiliary recording layer formation step.
 4. The method for manufacturing a magnetic disk according to claim 1, wherein a non-magnetic separation layer is interposed between the granular magnetic recording layer and the auxiliary recording layer.
 5. The method for manufacturing a magnetic disk according to claim 4, wherein the granular magnetic recording layer is formed of two or more layers. 